Tuberculosis
Conditions
Keywords
Tuberculosis, vaccine, nasal immunization
Brief summary
The purpose of this study is to determine whether a subunit tuberculosis vaccine given as two nasal immunizations composed of a hybrid protein antigen from M. tuberculosis virus mixed with a toxoid adjuvant, causes untoward adverse reactions when administered to healthy adult volunteers. Both subjects who have not received Bacillus Calmette-Guerin (BCG) and subjects who have already received BCG will be enrolled. An initial evaluation of immune responses to the vaccine will also be undertaken.
Detailed description
The purpose of this study is to determine whether a subunit tuberculosis vaccine given as two nasal immunizations composed of a hybrid protein antigen from M. tuberculosis virus mixed with a toxoid adjuvant, causes untoward adverse reactions when administered to healthy adult volunteers. Both subjects who have not received BCG and subjects who have already received BCG will be enrolled. An initial evaluation of immune responses to the vaccine will also be undertaken using flow cytometry to enumerate antigen specific IFNg containing T cells; ELISPOT to determine IFNg secreting antigen specific T cells; serology and nasal wash antibody.
Interventions
BIOLOGICALAg85B-ESAT6 fusion protein H1
100 ug H1 antigen in BCG naive subjects
Sponsors
Statens Serum Institut
Novartis Vaccines
European Union
St George's, University of London
Study design
Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to 55 Years
Healthy volunteers
Yes
Inclusion criteria
* Signed informed consent * Healthy, based on medical examination at inclusion * Male or female subjects, aged between 18 and 55 years * Willing and likely to be able to comply with the trial procedures * Prepared to grant authorized persons access to their medical records Additional inclusion criterion for BCG-non-vaccinated subjects: * BCG-non-vaccinated (i.e., absence of a BCG-scar) * Negative Mantoux skin test Additional inclusion criterion for BCG-vaccinated subjects: * BCG-vaccinated (i.e., presence of a BCG-scar)
Exclusion criteria
* History of TB or known exposure to TB * Radiological findings on chest X ray compatible with previous or current infection with tuberculosis * Positive QuantiFERON® TB-Gold test Evidence of previous, current or latent tuberculosis * Evidence of previous, current or latent tuberculosis * History of severe organ-system diseases * Known hypersensitivity to any of the vaccine components * History of allergic disorders * Vaccinated with other vaccine within 3 months before first vaccination * Congenital and/or acquired immune diseases * Administration of systemic immune modulating drugs (steroids, immunosuppressive drugs or immunoglobulin) within 3 months before the first vaccination (topical steroids not included) * Autoimmune diseases * HIV, HBV and HCV sero-positive * Established diagnosis of a neurological or neuromuscular disease, and specifically any history of abnormality with respect to sense of smell (olfactory nerve dysfunction), or previous or current facial nerve paralysis * Congenital or acquired abnormalities or disorders related to nasal and nasopharyngeal cavities * Current use of any medication taken through the nasal/inhalatory route including cocaine or other drugs * Laboratory parameters outside of normal ranges considered clinically significant * Pregnant according to urine pregnancy test * Females not willing to use contraceptives or who are breastfeeding * Intake of trial medication in other clinical trials within 6 months of the first vaccination
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To evaluate the safety profile (medical examinations, adverse events and laboratory safety tests) of a nasal TB subunit vaccine with and without adjuvant given as two doses with 2 months interval. | 8 months |
Secondary
| Measure | Time frame |
|---|---|
| To evaluate the cell mediated and humoral immunogenicity profile of a nasal TB subunit vaccine with and without adjuvant, given as two doses with 2 months interval. | 8 months |
Countries
United Kingdom
Outcome results
None listed